Palladium‐Catalyzed One‐Pot Coupling / Cyclization through Mo(CO) 6  as the Carbon Monoxide Donor: Synthesis of Quinazolinones | Zendy

Tao ShouWei | Zendy; Liu RuiQing | Zendy; Zhou JingYa | Zendy; Zhu YongMing | Zendy

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Palladium‐Catalyzed One‐Pot Coupling / Cyclization through Mo(CO) 6 as the Carbon Monoxide Donor: Synthesis of Quinazolinones

Author(s) -

Tao ShouWei,

Liu RuiQing,

Zhou JingYa,

Zhu YongMing

Publication year - 2020

Publication title -

chemistryselect

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 34

ISSN - 2365-6549

DOI - 10.1002/slct.202002111

Subject(s) - quinazolinone , palladium , carbon monoxide , aryl , catalysis , substrate (aquarium) , functional group , coupling (piping) , chemistry , combinatorial chemistry , coupling reaction , organic chemistry , materials science , metallurgy , alkyl , oceanography , polymer , geology

An efficient and rapid one‐pot synthesis of quinazolinone via a three‐component carbonylative coupling of 2‐aminobenzamide or 2‐aminobenzonitrile, Mo(CO) 6 and aryl bromides has been developed recently. This method provide a new way to synthesize quinazolinone which has a wide substrate scope, good functional group tolerance and mild reaction condition.

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